About
# Associate Medical Writer ## About the Role Clario, a part of Thermo Fisher Scientific, is a global leader in endpoint data solutions for clinical trials. With more than five decades of experience, the company combines deep scientific expertise with cutting-edge imaging, eCOA, motion, cardiac, and respiratory technologies to generate high-quality clinical evidence. Over 30,000 trials across 100+ countries have benefited from Clario’s solutions, contributing to more than 70% of FDA drug approvals since 2015. Clario’s purpose - to transform lives by unlocking better evidence - drives a culture of innovation, collaboration, and relentless focus on patient outcomes. The **Associate Medical Writer** role sits within the Medical Imaging team and offers a unique entry point for fresh talent eager to build a career at the intersection of medical writing, clinical research operations, and imaging science. You will report to senior medical writers and project leads, responsible for creating, reviewing, and maintaining a wide range of study-specific documentation that underpins successful trial execution. This position provides exposure to cross-functional teams, regulatory standards, and real-world clinical data, making it an ideal springboard for a long-term career in medical communications or clinical operations. ## Key Responsibilities - Support study startup by drafting, organizing, and curating Medical Writing and Communications documents such as Site Manuals, labels, and study-specific forms. - Review protocols and imaging requirements to ensure accurate interpretation of procedures, schedules, and operational needs. - Create, update, and finalize study documentation, including supporting forms, labels, and communication materials. - Develop and maintain compliance artifacts like Notes to File, amendment impact assessments, and corrective action records. - Generate source documentation and electronic clinical forms that align with operational requirements. - Prepare meeting agendas, minutes, and action-item logs for study startup and project meetings. - Assist in maintaining Medical Communications resources, databases, web content, and document repositories. - Participate in project close-out activities, ensuring proper archiving per regulatory and company standards. - Contribute to SOPs, work instructions, templates, and training material development. - Track document status, maintain databases, and provide guidance to project teams on documentation processes. ## Requirements - Strong skills in medical writing and clinical trial documentation. - Familiarity with regulatory compliance and medical imaging basics. - Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook. - Excellent attention to detail and proofreading capabilities. - Effective time management and cross-functional collaboration skills. ## Benefits - Work alongside world-class scientists and technologists. - Gain hands-on experience with high-impact clinical studies. - Benefit from a supportive environment that encourages continuous learning, professional certifications, and global mobility. - Enjoy competitive compensation and flexible remote work options. - Follow a clear career roadmap with opportunities for progression into roles such as Senior Medical Writer, Lead Medical Writer, or Medical Communications Manager.
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